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Determination of Lovastatin and Its Active Metabolites in Human Plasma with High Performance Liquid Chromatography-tandem Mass Spectrometry
Author(s): LIAO Dong-xue, QIN Yong-ping, GONG Xiao-li, LIANG Mao-zhi, YU Qin, NAN Feng, XIANG Jin
Pages: 730-
733
Year: 2009
Issue:
4
Journal: Journal of Sichuan University(Medical Science Edition)
Keyword: 高效液相色谱-串联质谱法; 洛伐他汀; 血药浓度; 代谢物; 洛伐他汀酸;
Abstract: 目的 建立高效液相色谱-串联质谱法(LC-MS/MS)测定人血浆中洛伐他汀及其活性代谢物洛伐他汀酸的浓度.方法 样品用乙酸乙酯∶二氯甲烷(体积比为1∶1)提取浓集后进样,色谱柱为Phenomenex Gemini C18(50×3 mm, 3 μm),流动相为乙腈-水(85∶15).质谱采用ESI离子源MRM模式检测,以辛伐他汀为内标,按内标法定量. 洛伐他汀、洛伐他汀酸和内标的检测离子对分别为质荷比(m/z)427.4→325.4、445.4→343.4和436.4→325.4.结果 洛伐他汀在0.031~64 μg/L范围内线性关系良好(r=0.9987),最低定量限为0.031 μg/L,方法 回收率在96%~102%之间,日内、日间精密度相对标准偏差(RSD)分别小于5.3%及9.3%.结论 本文建立的方法 准确、灵敏,可用于洛伐他汀血药浓度测定及药代动力学研究.
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